WordNet

small room in which a monk or nun lives (同)cubicle
a device that delivers an electric current as the result of a chemical reaction (同)electric cell
a room where a prisoner is kept (同)jail cell, prison cell
(biology) the basic structural and functional unit of all organisms; they may exist as independent units of life (as in monads) or may form colonies or tissues as in higher plants and animals
any small compartment; "the cells of a honeycomb"
a small unit serving as part of or as the nucleus of a larger political movement (同)cadre
of or relating to the bones of the fingers or toes

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出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2016/02/21 21:49:57」(JST)

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Trps1 deficiency inhibits the morphogenesis of secondary hair follicles via decreased Noggin expression.

Sun Y1, Nakanishi M2, Sato F2, Oikawa K2, Muragaki Y3, Zhou G4.
Biochemical and biophysical research communications.Biochem Biophys Res Commun.2015 Jan 16;456(3):721-6. doi: 10.1016/j.bbrc.2014.12.039. Epub 2014 Dec 13.
A representative phenotype of patients with tricho-rhino-phalangeal syndrome (TRPS) is sparse hair. To understand the developmental defects of these patient's hair follicles, we analyzed the development of hair follicles histologically and biochemically using Trps1 deficient (KO) mice. First, we com
PMID 25514040

Yokouchi M1, Arishima Y2, Nagano S3, Shimada H2, Nakamura S2, Setoguchi T4, Kawamura I2, Ishidou Y5, Komiya S6.
The Journal of foot and ankle surgery : official publication of the American College of Foot and Ankle Surgeons.J Foot Ankle Surg.2014 Dec 5. pii: S1067-2516(14)00452-9. doi: 10.1053/j.jfas.2014.09.023. [Epub ahead of print]
Giant cell tumor of the bone is a benign, but locally aggressive, primary bone tumor of unknown origin. It most commonly occurs in the long bones and is only rarely found in the phalangeal bones, such as the distal phalanx of the foot. In our review of English-language published studies, only 4 othe
PMID 25488596

Mutations Affecting the BHLHA9 DNA-Binding Domain Cause MSSD, Mesoaxial Synostotic Syndactyly with Phalangeal Reduction, Malik-Percin Type.

Malik S1, Percin FE2, Bornholdt D3, Albrecht B4, Percesepe A5, Koch MC3, Landi A6, Fritz B3, Khan R7, Mumtaz S7, Akarsu NA8, Grzeschik KH9.
American journal of human genetics.Am J Hum Genet.2014 Dec 4;95(6):649-59. doi: 10.1016/j.ajhg.2014.10.012. Epub 2014 Nov 13.
Mesoaxial synostotic syndactyly, Malik-Percin type (MSSD) (syndactyly type IX) is a rare autosomal-recessive nonsyndromic digit anomaly with only two affected families reported so far. We previously showed that the trait is genetically distinct from other syndactyly types, and through autozygosity m
PMID 25466284